Canonical Allele Identifier: PA2826463711
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483753
ClinVar RCV Id: RCV000563990 RCV002528140 RCV003451252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile290Lys
CA346733264
NM_001258281.1:c.869T>A